[Cytogenesis and histogenesis of malignant and semimalignant bone tumors].

A Roessner, E Grundmann
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Abstract

Our present knowledge about bone tumors is still in need of a convincing cytohistogenetic concept that would support the adequate differentiation and classification of different tumor types. The modern therapeutic approach must rely on subtle diagnostis using preferably cyto- and histomorphologic criteria. The present study depends on a considerable number of malignant and semimalignant bone tumors which were analysed by several modern investigative methods. Based on these results, we intend to find the answers to some problems of cytogenesis and histogenesis of bone tumors. Comparison and correlation of our findings with the results of other authors is attempted with the objective to propose an overall histogenetic concept of bone tumors in consideration of the known data and hypotheses. Our material comprises 85 malignant and semimalignant bone tumors. The following tumor types are discussed on the basis of cases from our collection (numbers in brackets): "Conventional" highly malignant osteosarcoma (32), parosteal and periosteal osteosarcoma (2), telangiectatic osteosarcoma (2), small cell osteosarcoma (1), small cell sclerosing osteosarcoma (2), histiocytic osteosarcoma (1), Ewing's sarcoma (15), "conventional" chondrosarcoma (7), dedifferentiated chondrosarcoma (2), mesenchymal chondrosarcoma (1), giant cell tumor (12), malignant fibrous histiocytoma of bone (5), fibrosarcoma of bone (3), The results of conventional light and electron microscopy, but also of enzyme histochemistry and autoradiography were included in the definitive classification by both histologic and cytologic criteria. In addition, different collagen types present in the ground substance of these tumors were studied by immunofluorescence microscopy; in anaplastic tumors of high malignancy the intermediate filaments of the cytoskeleton were further subjected to immunohistochemical analysis. The concept resulting from these studies may be briefly summarized as follows: The stem cell of conventional, highly malignant osteosarcoma is a stromal cell of the skeletal system, which is undergoing neoplastic transformation. At first this cell fails to show any sign of collagen synthesis, the activity of alkaline phosphatase is not increased. Of a primarily anaplastic nature, this tumor cell may differentiate in several directions: in osteoblastic differentiation, the cell will produce predominantly collagen type I, and alkaline phosphatase activity will increase. During fibroblastic differentiation we observe an increased synthesis of collagen type III, but alkaline phosphatase activity is not raised.(ABSTRACT TRUNCATED AT 400 WORDS)

[恶性和半恶性骨肿瘤的细胞发生和组织发生]。
我们目前对骨肿瘤的认识仍然需要一个令人信服的细胞组织遗传学概念,以支持不同类型肿瘤的充分分化和分类。现代的治疗方法必须依赖于细微的诊断,最好使用细胞和组织形态学标准。目前的研究依赖于相当数量的恶性和半恶性骨肿瘤,这些肿瘤是用几种现代调查方法分析的。在此基础上,探讨骨肿瘤细胞发生和组织发生的一些问题。我们试图将我们的发现与其他作者的结果进行比较和关联,目的是在考虑已知数据和假设的情况下提出骨肿瘤的整体组织遗传学概念。我们的材料包括85例恶性和半恶性骨肿瘤。根据我们收集的病例,讨论了以下肿瘤类型(括号内的数字):“常规”高度恶性骨肉瘤(32例)、骨旁和骨膜骨肉瘤(2例)、毛细血管扩张性骨肉瘤(2例)、小细胞骨肉瘤(1例)、小细胞硬化性骨肉瘤(2例)、组织细胞性骨肉瘤(1例)、尤文氏肉瘤(15例)、“常规”软骨肉瘤(7例)、去分化软骨肉瘤(2例)、间充质软骨肉瘤(1例)、巨细胞瘤(12例)、骨恶性纤维组织细胞瘤(5例)、骨纤维肉瘤(3例)、常规光镜和电子显微镜的结果,以及酶组织化学和放射自显影的结果都包括在组织学和细胞学标准的明确分类中。此外,用免疫荧光显微镜研究了这些肿瘤基质中存在的不同胶原类型;在高度恶性间变性肿瘤中,细胞骨架的中间纤维进一步进行免疫组织化学分析。从这些研究中得出的概念可以简单概括如下:常规的高度恶性骨肉瘤的干细胞是一种正在发生肿瘤转化的骨骼系统基质细胞。起初,这个细胞没有表现出任何胶原合成的迹象,碱性磷酸酶的活性没有增加。主要是间变性,这种肿瘤细胞可能向几个方向分化:在成骨细胞分化中,细胞将主要产生I型胶原,碱性磷酸酶活性将增加。在成纤维细胞分化过程中,我们观察到III型胶原合成增加,但碱性磷酸酶活性没有提高。(摘要删节为400字)
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